| Tag | Content |
|---|
EnhancerAtlas ID | HS184-13652 | Organism | Homo sapiens | Tissue/cell | T47D | Coordinate | chr17:43822560-43824100 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| ZNF263 | MA0528.1 | chr17:43823953-43823974 | GGTGGAGACAGAGGAAGAGGA | + | 6.24 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr17 | 43823012 | 43823635 | | chr17 | 43822727 | 43822792 |
| Enhancer Sequence | GTGCTATTTT ATGTGTTATG CTCTGAGGGT TCATTCATGC AGGCAGTGTG TAATGAGCAC 60
TCGCTACATG CCAGGCCCTG AGGACAGAGC AGTAAAGGAG CCGATGTCCT TGCCTGCATG 120
GAGGTCCCAT CCAAGTGAGG AGACAGTTAA AATGCAAACA CAGCTGCACG ATATTGTCAG 180
GTGATGCTTT GTGCTGAGAA GGATGAAGCG GTAGGGGGGA TGGAGAGAGT GGGGTGGGTG 240
GGGTGCTATT TCAGATTGAA GGGTCAGCGA GGTCCTGCAG AAGAGCTTCA ATTTAAATGG 300
AAGCCACCAC TGAGAACGAA TAGGGGGGAT TTGGGGCATC CCAGGTGAGG AGTGGGATTC 360
AGAAAGAAGA ATTCCTTGAC ATCCCAGGCT CCTTGGTGAG CCAGTGGGGA CACATTCTGC 420
TTGTCATCAA AGTGAATTAC AAACTCATCC AGCTCAGAGC CTCTGCCAGA GCCATCTGGG 480
CTGCAGTGGC CTCTTTCAAA GAAAAGAGTT CGCCAACAAG AAAGCGGCAC GGCATCCTGA 540
TGAGGACTGG GGCTTTAGAG TTCTGGGCAG AAACGTGTTG AAATCCCAGC TCAGGCATGA 600
TTGAGGTTCA TGTCTTAATC CCTGAGAGCT TTGGTTTCTT TATATGTAGT CGGGAATGAT 660
AACAGTGCTT CTCCCAGAGG GTTGTTGTAA GTCTTCAAAG AAACAGCCTG TGTAAAGTGC 720
TGAGCACAGA TAAACAGTGG CCTTTACTGC CATTGTCATT CTCTTAGCTC CCAGTGGGGT 780
TCTTTGCTTC TCTTTCATTC ATTCCACAAT AACTGAGCAC CTACTCATTG TCAGGCTCTA 840
GATGCTAGGG TACCCAGAGG AGGAACACCT AAGCTATCCA AATGTGAGCC AGAGAGTGCA 900
CCCATCCAAG AGGCAGGGCC CTGGGCATGC ATTCCTGCCA TTCCAGCTGT GTGAACTTGG 960
CCATGTGGTT TCATCGCCCT GGGCCTCAGC TTTCCCCACT GCAAATAGAG GGCTCAGCTT 1020
GCCAATCACT GGGTGATTCT CCTGCTGAGC TCCTGGGCTG AGGCTGGGGC ACAACTGTGG 1080
AGGGAGCATC TGTAGCCCCA GGTGACCTGA GCCTCAGAGA AAGCTAGCCT GCCTGGCCCG 1140
GAGGCTCTGC TGGGAGTGGG GTGGGAAGAA GCCCATGTGC TCGGAAATGG GCCAGGGTCA 1200
GTGCTGGGGC CTGTCGCCCC CAAGGACCCT CCCACATCAA CCAGAGCTCC TCATGGGGAG 1260
GCAGAGGGTA CAGCCGCTGA ACGTGCCTTC CCAGGAGAAG CTTGAAGTGT ACTCAGGATC 1320
TTGGCAGGCA TCGGGGTTCT GAGGGGTCGT AAGAGGGGCC GCTAGGGACA GGGCTCCAGA 1380
GAGGCCTGAT GAAGGTGGAG ACAGAGGAAG AGGATATCTA GGAGAAGGGG TTTGTCCTAT 1440
TTCCTCCCAA GTGCCACTTG CACTTCTAGT GCTGGGAGTC ATTCATTATA CAGATGATTA 1500
TACAGTCATT CATTATACAG ATGGCTGGGG CCACCACACT 1540
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